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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Certain genetic variations are linked to hair loss in Mexican men.

The document concludes that targeting the androgen receptor may be a promising breast cancer treatment, especially for certain types.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

The conclusion is that skin and hair patterns are formed by a mix of cell activities, molecular signals, and environmental factors.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

CDP is crucial for lung and hair follicle cell development.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A male with aromatase deficiency improved bone health with estradiol treatment.

The document explains how to identify different hair problems using a microscope.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

No link found between new male baldness genes and female hair loss.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

ERβ has potential in treating prostate cancer and neurodegenerative diseases, but human studies are needed before clinical use.